madcam1[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3907418	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 496,724-497,515 , GRCh38.p12 chr19: 496,724-497,515	MADCAM1
nsv3891938	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 474,588-496,670 , GRCh38.p12 chr19: 474,588-496,670	MADCAM1, CIMAP1D
nsv3904631	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 496,724-529,004 , GRCh38.p12 chr19: 496,724-529,004	MADCAM1, TPGS1, 1 more genes
nsv3905884	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 499,978-529,004 , GRCh38.p12 chr19: 499,978-529,004	MADCAM1, TPGS1, 1 more genes
nsv3903889	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 474,588-541,685 , GRCh38.p12 chr19: 474,588-541,685	MADCAM1, CDC34, 3 more genes
nsv3898347	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 467,701-519,619 , GRCh38.p12 chr19: 467,701-519,619	MADCAM1, CIMAP1D, 2 more genes
nsv3898580	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 460,883-512,568 , GRCh38.p12 chr19: 460,883-512,568	MADCAM1, CIMAP1D, 3 more genes
nsv3894779	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 474,588-525,739 , GRCh38.p12 chr19: 474,588-525,739	MADCAM1, CIMAP1D, 2 more genes
nsv3895601	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 474,645-519,619 , GRCh38.p12 chr19: 474,645-519,619	MADCAM1, TPGS1, 2 more genes
nsv3908727	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 474,588-518,841 , GRCh38.p12 chr19: 474,588-518,841	MADCAM1, CIMAP1D, 2 more genes
nsv3894677	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 473,932-517,284 , GRCh38.p12 chr19: 473,932-517,284	MADCAM1, CIMAP1D, 2 more genes
nsv3909604	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 474,645-509,267 , GRCh38.p12 chr19: 474,645-509,267	MADCAM1, TPGS1, 2 more genes
nsv3906850	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 474,645-508,220 , GRCh38.p12 chr19: 474,645-508,220	MADCAM1, TPGS1, 2 more genes
nsv3898649	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 478,060-508,626 , GRCh38.p12 chr19: 478,060-508,626	MADCAM1, CIMAP1D, 2 more genes
nsv3895626	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 495,722-525,739 , GRCh38.p12 chr19: 495,722-525,739	MADCAM1, MADCAM1-AS1, 1 more genes
nsv6315510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,911-1,319,319 , GRCh38.p12 chr19: 260,911-1,319,320	MADCAM1, LOC101928450, 66 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	MADCAM1, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	MADCAM1, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	MADCAM1, LENG8, 2408 more genes
nsv3924102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622	MADCAM1, POLR2E, 283 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 48

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Number of Variants: 20

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Supplemental Content

Find related data

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